向 智里 | Faculty Of Pharmaceutical Sciences Osaka University
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概要
関連著者
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向 智里
Faculty of Pharmaceutical Sciences, Kanazawa University
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向 智里
Faculty Of Pharmaceutical Sciences Osaka University
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向 智里
金沢大学薬学部
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花岡 美代次
Faculty Of Pharmaceutical Sciences Osaka University
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花岡 美代次
Faculty Of Pharmaceutical Sciences Kanazawa University
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花岡 美代次
Faculty of Pharmaceutical Sciences, Kanazawa University
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花岡 美代次
金沢大学薬学部
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花岡 美代次
Institute Of Natural Medicine University Of Toyama
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吉田 修治
Faculty of Pharmaceutical Sciences, Kanazawa University
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趙 元済
Faculty of Pharmaceutical Sciences, Kanazawa University
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趙 元済
Faculty Of Pharmaceutical Sciences Kanazawa University
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吉田 修治
Faculty Of Pharmaceutical Sciences Kanazawa University
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田村 恭光
Faculty Of Pharmaceutical Sciences Osaka University
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池田 正澄
Faculty of Pharmaceutical Sciences, Osaka University
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池田 正澄
Kyoto Pharmaceutical University
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荒田 義雄
Faculty Of Pharmaceutical Sciences Kanazawa University
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山岸 喬
Natural Products Laboratory Division Of Medicinal Chemistry And Natural Products School Of Pharmacy
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山岸 浩
Faculty Of Pharmaceutical Sciences Kanazawa University
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安田 信吾
金沢大・薬
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詠 和良
Faculty of Pharmaceutical Sciecnes, Kanazawa University
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詠 和良
Faculty Of Pharmaceutical Sciecnes Kanazawa University
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安田 信吾
Faculty of Pharmaceutical Sciences, Kanazawa University
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丸谷 真理
Faculty of Pharmaceutical Sciences, Kanazawa University
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丸谷 真理
Faculty Of Pharmaceutical Sciences Kanazawa University
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桜井 俊一郎
北陸製薬株式会社中央研究所研究開発本部
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三平 亜土
Faculty of Pharmaceutical Sciences, Kanazawa University
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趙 元剤
Faculty of Pharmaceutical Sciences, Kanazawa University
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杉浦 洋子
Faculty of Pharmaceutical Sciences, Kanazawa University
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笛木 司
Faculty of Pharmaceutical Sciences, Kanazawa University
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橋詰 聡
Faculty of Pharmaceutical Sciecnes, Kanazawa University
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鈴木 公正
Faculty of Pharmaceutical Sciences, Kanazawa University
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趙 元剤
Faculty Of Pharmaceutical Sciences Kanazawa University
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岡嶋 恵子
Faculty of Pharmaceutical Sciences, Kanazawa University
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杉浦 洋子
Faculty Of Pharmaceutical Sciences Kanazawa University
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大島 武
Faculty Of Pharmaceutical Sciences
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三平 亜土
Faculty Of Pharmaceutical Sciences Kanazawa University
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池田 裕之
The Institute of Physical and Chemical Research
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櫻井 俊一郎
Faculty of Pharmaceutical Sciences, Kanazawa University
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BAYOMI Said
Faculty of Pharmacy, University of Mansoura
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橋詰 聡
Faculty Of Pharmaceutical Sciecnes Kanazawa University
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岡嶋 恵子
Faculty Of Pharmaceutical Sciences Kanazawa University
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Bayomi Said
Faculty Of Pharmaceutical Sciences Osaka University
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濱中 伊都子
Faculty of Pharmaceutical Sciences, Kanazawa University
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関 和恵
Faculty of Pharmaceutical Sciences, Kanazawa University
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濱中 伊都子
Faculty Of Pharmaceutical Sciences Kanazawa University
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櫻井 俊一郎
Faculty Of Pharmaceutical Sciences Kanazawa University
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鈴木 公正
Faculty Of Pharmaceutical Sciences Kanazawa University
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関 和恵
Faculty Of Pharmaceutical Sciences Kanazawa University
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笛木 司
Faculty Of Pharmaceutical Sciences Kanazawa University
著作論文
- Erythro-Selective Aldol Reaction of Tricarbonyl(η^6-o-trialkylsilylbenzaldehyde)chromium(0) Complexes with Cyclic Ketene Silyl Acetals
- Chemical Transformation of Protoberberines. XVII. Biomimetic Introduction of an Oxy Functionality at the C-10 Position in the Benzo[c]phenanthridine Skeleton : Synthesis of 2,3,7,8,10-Pentaoxygenated Benzo[c]phenanthridine Alkaloids, Chelilutine and Sangu
- A FIRST TOTAL SYNTHESIS OF (±)-AMBININE
- Chemical Transformation of Protoberberines. XVI. Regioselective Introduction of an Oxy Functionality at the C_-Position of the Benzo[c]phenanthridine Skeleton : A Convenient Synthesis of Macarpine from Oxychelirubine
- Trimethylsilyl Trifluoromethanesulfonate-Catalyzed Aldol Reaction of Various Aldehydes with Silyl Enol Ethers
- A NOVEL DIASTEREOSELECTIVITY IN THE ALDOL REACTION OF CYCLIC KETENE SILYL ACETALS WITH COBALT-COMPLEXED AND UNCOMPLEXED PROPYNALS
- Chemical Transformation of Protoberberines. XV. : A Novel and Efficient Method for the Introduction of Alkyl Groups on the C-13 Position in the Protoberberine Skeleton
- A NOVEL AND BIOMIMETIC SYNTHESIS OF CHELILUTINE AND SANGUILUTINE
- Chemical Transformation of Protoberberines. V. Photochemical Valence Isomerization of Berberinephenolbetaines to 8,14-Cycloberbines, Versatile Aziridine Derivatives for a Novel and Efficient Entry to Spirobenzylisoquinolines and Benzindenoazepines
- Chemical Transformation of Protoberberines. XIII. A Novel and Efficient Synthesis of Antitumor Benzo[c]phenanthridine Alkaloids, Nitidine and Fagaronine(Organic,Chemical)
- Chemical Transformation of Protoberberines. XI. A Novel Synthesis of 2,3,10,11-Tetraoxygenated Protoberberine Alkaloids from Corresponding 2,3,9,10-Tetraoxygenated Protoberberine Alkaloids(Organic,Chemical)
- SYNTHESIS OF FAGARIDINE, A PHENOLIC BENZO [c] PHENANTHRIDINE ALKALOID
- TRANSFORMATION OF PROTOBERBERINES INTO SPIROBENZYLISOQUINOLINES. STEREOSELECTIVE CONVERSION OF COPTISINE INTO (±)-OCHROBIRINE
- Photolysis and Thermolysis of 3-Diazothiochroman-4-one and Related Compounds
- Synthesis, Stereochemistry, and Rearrangement of N-Tosylsulfilimines and (Bismethoxycarbonyl) methylides of 1,4-Dimethylthioxanthene and Its 9-Alkyl Derivatives
- Chemical Transformation of Protoberberines. III. Convenient Synthesis of 8-Methoxyberberinephenolbetaine by Photooxygenation of Berberine. A Novel Conversion of Berberine into (±)-Ophiocarpine, (±)-Epiophiocarpine, (±)-α-Hydrastine, and (±)-β-Hydrastine
- Chemical Transformation of Protoberberines. I. Conversion of Tetrahydroberberine and Dihydroberberine into Noroxyhydrastinine by Photooxygenation